Literature DB >> 10401004

Defective copper-induced trafficking and localization of the Menkes protein in patients with mild and copper-treated classical Menkes disease.

L Ambrosini1, J F Mercer.   

Abstract

Menkes disease is an X-linked disorder of copper metabolism. An overall copper deficiency reduces the activity of copper-dependent enzymes accounting for the clinical presentation of affected individuals. The Menkes gene product (MNK) is a P-type ATPase and is considered to be the main copper efflux protein in most cells. The protein is located primarily at the trans -Golgi network (TGN), but relocalizes to the plasma membrane in elevated copper conditions to expel the excess copper from the cell. Here we report the first missense mutation which causes mild Menkes disease, a mutation in a successfully copper-treated classical Menkes patient and the effect of each mutation on the localization of MNK within the cell. Using western blot analysis, MNK was detectable in cells from both patients, but appeared to be mislocalized in the treated case. In the mild Menkes patient, the protein appeared to be located in the TGN but failed to redistribute towards the cell periphery in response to copper. This is the first description of a mutation in a Menkes patient which affects the trafficking of MNK, and the loss of this process is consistent with the clinical phenotype.

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Year:  1999        PMID: 10401004     DOI: 10.1093/hmg/8.8.1547

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  20 in total

1.  The molecular and genetic base of congenital transport defects.

Authors:  J F Desjeux
Journal:  Gut       Date:  2000-05       Impact factor: 23.059

2.  A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease.

Authors:  S L Dagenais; A N Adam; J W Innis; T W Glover
Journal:  Am J Hum Genet       Date:  2001-06-26       Impact factor: 11.025

Review 3.  Diagnosis of Wilson disease in young children: molecular genetic testing and a paradigm shift from the laboratory diagnosis.

Authors:  Jeong Kee Seo
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2012-12-31

Review 4.  ATP7A-related copper transport diseases-emerging concepts and future trends.

Authors:  Stephen G Kaler
Journal:  Nat Rev Neurol       Date:  2011-01       Impact factor: 42.937

5.  The mild form of menkes disease: a 34 year progress report on the original case.

Authors:  M C Tchan; B Wilcken; J Christodoulou
Journal:  JIMD Rep       Date:  2012-10-13

6.  Evidence that translation reinitiation leads to a partially functional Menkes protein containing two copper-binding sites.

Authors:  Marianne Paulsen; Connie Lund; Zarqa Akram; Jakob R Winther; Nina Horn; Lisbeth Birk Møller
Journal:  Am J Hum Genet       Date:  2006-06-05       Impact factor: 11.025

Review 7.  Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

Authors:  P de Bie; P Muller; C Wijmenga; L W J Klomp
Journal:  J Med Genet       Date:  2007-08-23       Impact factor: 6.318

8.  Differences in ATP7A gene expression underlie intrafamilial variability in Menkes disease/occipital horn syndrome.

Authors:  Anthony Donsante; Jingrong Tang; Sarah C Godwin; Courtney S Holmes; David S Goldstein; Alexander Bassuk; Stephen G Kaler
Journal:  J Med Genet       Date:  2007-05-11       Impact factor: 6.318

9.  Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein.

Authors:  Byung-Eun Kim; Michael J Petris
Journal:  J Med Genet       Date:  2007-05-04       Impact factor: 6.318

10.  A comparison of the mutation spectra of Menkes disease and Wilson disease.

Authors:  Gloria Hsi; Diane W Cox
Journal:  Hum Genet       Date:  2003-10-25       Impact factor: 4.132

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